Not currently registered with FDA under this name

Richard Wolf Medical Instruments Corp.

Rosemont, IL, United States. Named as applicant on 1 dental 510(k) clearance between 1991 and 1991. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 11991–1991
Markets registered in: 24 registrations outside the US
Establishments: 0—

510(k) clearances per year, 1990–2026

Registered in 2 markets

Where regulators' registries name Richard Wolf Medical Instruments Corp. as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Applicant	Richard Wolf Medical Instruments Corp.	1 clearances	1991–1991	Below
South Korea	MFDS	Manufacturer	Richard Wolf Medical Instruments Corp.Richard Wolf Medical Instruments Corporation	4	2000–2020	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Richard Wolf Medical Instruments Corp. as the applicant.

Decided	510(k)	Device	Device type
24 Oct 1991	K911756	POSTERIOR NASAL EPISTAXIS INSTRUMENTS	ECB Air and/or Water Syringe Unit

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.